Ventris Intervertebral Body Fusion Device

Ventris Intervertebral Body Fusion Device is an FDA 510(k)-cleared medical device (K243386) manufactured by Acuity Surgical Devices, LLC. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 21, 2025. Regulation: 8.